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In contrast to the alkali charge and temperature, the charge of oxygen plays a less
important role, as long as sufficient oxygen is present in the oxygen delignification
system. It is agreed that an oxygen charge between 20 and 30 kg bdt–1 is sufficient
to avoid any oxygen-based limitation of the delignification process. In the
literature, different values for specific oxygen consumption per unit kappa number
reduction (DO2/Dkappa number) are reported. According to laboratory studies,
the oxygen consumption per unit kappa number reduction varies from 0.5 to
0.6 kg bdt–1 [54,55]. The evaluation of industrial oxygen delignification plants
revealed oxygen consumption values of 1.4 kg bdt–1 per unit kappa number
decrease for softwoods, and 1.6 kg bdt–1 for hardwoods [56]. In a dissolving pulp
mill using unbleached beech acid sulfite pulp, the oxygen consumption was calculated
from the quantity and composition of the exhaust gas from the blow tank of
the oxygen delignification stage [57]. A “helium tracer technique” was applied to
control the oxygen consumption [31].
From these measurements it can be concluded that the specific oxygen consumption
rate amounts to approximately 1.0 kg per unit of kappa number
decrease.
With increasing temperature, the utilization of oxygen increases without significantly
improving the delignification efficiency. Furthermore, it is reported that the
increased oxygen consumption parallels the increased loss of pulp yield.
On the basis of detailed material balances, the amount of oxygen consumed
during an industrial oxygen delignification process was estimated [58]. The study
of Salmela and Alen indicates that part of the oxygen bound to the reaction products
originates from alkali (about 13%), part from molecular oxygen (about 33%),
and the major part from the pulp (about 54%) itself. The specific consumption of
molecular oxygen needed for the oxidation reactions is, however, limited to 0.6–
1.0 kg bdt–1, which is in good agreement with the results obtained from laboratory
studies. An increase in the oxygen charge primarily induces increased oxidation
reactions with dissolved organic and inorganic compounds.
Unlike the oxygen charge, the oxygen pressure significantly influences the degradation
rate (see Section 7.3.4). Model compound studies using phenolic b-aryl
ether confirmed the pronounced effect of oxygen pressure on degradation rate
(Fig. 7.44).
Commercial oxygen delignification plants typically use pressures in the range
400 to 870 kPa with medium consistency systems applying higher pressures as
compared to high consistency plants [59]. However, there is a clear trend to
further increase oxygen pressure as high as technically feasible, especially in twostage
operations.
7.3 Oxygen Delignification 707
0 20 40 60 80
oxygen pressure: 0.4 MPa 0.6 MPa 1.1 MPa
Remaining â-arylether [%]
Reaction time [min]
Fig. 7.44 Influence of oxygen pressure on the degradation
rate of a phenolic b-aryl ether compound at pH 11 and 100 °C
(according to [39]).
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